Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0085614
Disease: First degree atrioventricular block
First degree atrioventricular block 		26 0 22 0.41 0 0
CUI: C0155707
Disease: Trifascicular block
Trifascicular block 		23 0 21 0.40 0 0
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding) 		23 0 21 0.40 0 0
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia 		24 0 21 0.40 0 0
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		28 0 22 0.39 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		39 0 23 0.35 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		51 0 24 0.31 0 0
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		13 0 13 0.26 0 0
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		96 0 29 0.25 0 0
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		12 0 12 0.24 0 0
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		12 0 12 0.24 0 0
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		13 0 12 0.24 0 0
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		13 0 12 0.24 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		66 0 22 0.23 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		40 0 14 0.18 0 0
CUI: C0039070
Disease: Syncope
Syncope 		119 0 25 0.17 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		18 0 8 0.13 0 0
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval 		13 0 7 0.12 0 0
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		104 0 17 0.12 0 0
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		24 4 8 0.12 2 0.22
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 7 0.12 2 0.14
CUI: C2931783
Disease: Amelogenesis imperfecta nephrocalcinosis
Amelogenesis imperfecta nephrocalcinosis 		19 0 7 0.11 0 0
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		41 0 9 0.11 0 0
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		105 0 15 0.11 0 0
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		23 4 7 0.11 2 0.22